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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01697605
Other study ID # CBGJ398X1101
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date October 19, 2012
Est. completion date February 7, 2019

Study information

Verified date March 2020
Source Novartis
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will evaluate safety and tolerability to determine the Maximum tolerated dose (MTD) and/or Recommended dose (RD).


Description:

This is a multi-center, open label, dose finding, phase I study of oral single agent BGJ398, administered on a continuous once and/or twice daily schedule.


Recruitment information / eligibility

Status Completed
Enrollment 9
Est. completion date February 7, 2019
Est. primary completion date February 7, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with advanced solid tumors with FGF-R alteration - Eastern Cooperative Oncology Group (ECOG) performance status 0-2 - Adequate organ function Exclusion Criteria: - Patients with untreated and/or symptomatic metastatic Central Nerve System (CNS) disease - Pregnant or nursing (lactating) women Other protocol-defined inclusion/exclusion criteria may apply.

Study Design


Related Conditions & MeSH terms

  • Tumor With Alterations of the FGF-R

Intervention

Drug:
BGJ398


Locations

Country Name City State
China Novartis Investigative Site Chengdu Sichuan
China Novartis Investigative Site Guangzhou
China Novartis Investigative Site Guangzhou Guangdong
Japan National Cancer Center Hospital East (NCEE) Kashiwa Chiba
Japan Novartis Investigative Site Kobe-shi Hyogo
Japan Nagoya University Hospital Nagoya-city Aichi
Japan Novartis Investigative Site Sayama Osaka
Japan Shizuoka Cancer Center Sunto-gun Shizuoka

Sponsors (1)

Lead Sponsor Collaborator
Novartis Pharmaceuticals

Countries where clinical trial is conducted

China,  Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence rate and category of dose limiting toxicities (DLTs) Maximum tolerated dose (MTD) and/or Recommended dose (RD) of single agent oral BGJ398 First cycle of 28 days
Secondary Frequency of all Adverse Events (AEs) and Serious Advers Events (SAEs) To characterize the safety and tolerability of oral BGJ398 From within 21 days of first treatment to 28 days after treatment discontinuation
Secondary Changes in hematology and chemistry values hematology and chemistry values From baseline to 28 days after treatment discontinuation
Secondary Assessments of physical examinations, vital signs and electrocardiograms (ECGs) Participants will be followed for the duration of treatment, an expected average of 24 weeks.
Secondary Time vs. concentration profiles To determine the pharmacokinetic (PK) profiles (Cmax, AUC, Tmax, T1/2, etc) of oral BGJ398 including known pharmacologically active metabolites 1 to 10 time points (0, 0.25, 1, 2, 3, 4, 6, 8, 12, 24 hours post-dose) up to 24 weeks
Secondary Preliminary anti-tumor activity Assessed based on RECIST version 1.1 Participants will be followed for the duration of treatment, an expected average of 24 weeks.
Secondary Best overall response (BOR) Assessed by investigator per RECIST version 1.1. BOR is the best response recorded until disease progression. Participants will be followed for the duration of treatment, an expected average of 24 weeks.
Secondary Overall response rate (ORR) Assessed by investigator per RECIST version 1.1. ORR is the proportion of patients with a best overall response of Complete Response (CR) or Partial Response (PR). Participants will be followed for the duration of treatment, an expected average of 24 weeks.
Secondary Progression-free survival (PFS) PFS is defined as the times from the date of first dose of BGJ398 to the date of the first documented disease progression, date of death due to any cause or until a new anticancer therapy is initiated, whichever occurs first. From date of end of treatment until the date of progression, or date of death, or starting date of a new anticancer therapy, assessed up to 100 months.
Secondary Duration of all Adverse Events (AEs) To characterize the safety and tolerability of oral BGJ398 From within 21 days of first treatment to 28 days after treatment discontinuation
Secondary Duration of Serious Advers Events (SAEs) To characterize the safety and tolerability of oral BGJ398 From within 21 days of first treatment to 28 days after treatment discontinuation
Secondary Severity of all Adverse Events (AEs) To characterize the safety and tolerability of oral BGJ398 From within 21 days of first treatment to 28 days after treatment discontinuation
Secondary Severity of all Serious Advers Events (SAEs) To characterize the safety and tolerability of oral BGJ398 From within 21 days of first treatment to 28 days after treatment discontinuation